Difference between revisions of "Part:BBa K3402050"
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This device is composed of promoter P<i>tef1</i> ([https://parts.igem.org/Part:BBa_K3402007# BBa_K3402007]), reporter gene <i>yeGFP</i> ([https://parts.igem.org/Part:BBa_K3402000# BBa_K3402000]), terminator T<i>syn7</i> ([https://parts.igem.org/Part:BBa_K3402001# BBa_K3402001]). | This device is composed of promoter P<i>tef1</i> ([https://parts.igem.org/Part:BBa_K3402007# BBa_K3402007]), reporter gene <i>yeGFP</i> ([https://parts.igem.org/Part:BBa_K3402000# BBa_K3402000]), terminator T<i>syn7</i> ([https://parts.igem.org/Part:BBa_K3402001# BBa_K3402001]). | ||
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− | [[Image:Report circuit-zzh.png|400px | + | [[Image:Report circuit-zzh.png|400px]] |
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 14:49, 25 October 2020
report circuit
This device is composed of promoter Ptef1 (BBa_K3402007), reporter gene yeGFP (BBa_K3402000), terminator Tsyn7 (BBa_K3402001).
Usage and Biology
The green fluorescent protein (yeGFP) gene can be used as reporter gene and express in Starmerella bombocola. We want to test if the yeGFP can express in Starmerella bombocola, so we connected this device. Besides, the hygromycin resistance gene (hph) was built into the plasmid as the marker gene to determine if the transformation is successful. Two homologous arms are used to intsert this gene into PXA1 gene.
As a result, the expression of the yeGFP in Starmerella bombocola is completed. Finally, we can link different promoters to yeGFP to know the strength of promoters by testing different fluorescence intensity of different promoters.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1051
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1492